- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03871374
Factors Affecting Salt Intake in Young Adults
Study Overview
Status
Conditions
Detailed Description
Hypertension is a major cause of cardiovascular disease (CVD) and overall mortality. High dietary salt intake is a major risk factor for hypertension estimated to be responsible for one in ten deaths from CVD events. Salt consumption worldwide and in the UK exceeds the recommendations. One of the main determinants of food intake, and potentially salt, is taste which may be genetically determined. Research exploring the associations between genetics, salt taste and salt intake is scarce. Better understanding of these associations would be of specific interest in younger populations as it has been shown that it is the young adults that have higher preference for salty taste and consequently salt intake. Therefore, the aim of this study is to explore the associations between genetics, salt taste perception and salt intake in young UK adults.
One hundred participants (18-35 years) will be recruited. Salt taste thresholds will be identified using the British Standards Institution sensory analysis method (BS ISO 3972:2011) and preference for salty taste by rating the pleasantness and bitterness of six tomato soups with differing salt concentrations. Salt intake will be measured using five step multiple pass 24-hour recall completed via online platform (Online surveys) for one day of the week and one weekend day. Participants will be genotyped for genetic variants in the SCNN1B and TRPV1 genes coding for ion channels expressed in taste cells.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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London, United Kingdom, TW14SX
- St Mary's University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Males or females, aged 18-35 years and healthy.
Exclusion Criteria:
- Current stage 1 or 2 hypertension
- Current or recent (less than one month prior to screening visit) use of antihypertensive medications or medications that affect BP
- Secondary hypertension
- History of cardiovascular disease, including myocardial infarction, congestive heart failure, stroke, and peripheral arterial disease
- Chronic kidney failure
- Peptic ulcer disease requiring treatment during the previous two years
- Currently pregnant women
- Underweight (BMI<18.5 kg/m2) and obese (BMI>30 kg/m2)
- Currently adhering to a low sodium diet
- Any illness that permanently alters taste
- Inability or unwillingness to participate or sign informed consent form
- Food allergy
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Salt intake
Time Frame: 2 days observation
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Dietary salt intake - two 24-hour recalls
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2 days observation
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SMEC_2018-19_007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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